Canonical Allele Identifier: CA1619467728
Gene: NOTCH4 HGNC NCBI

Linked Data

dbSNP Id: rs1788431777
gnomAD v4: 6-32202670-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32202670T>C , CM000668.2:g.32202670T>C GRCh38
NC_000006.11:g.32170447T>C , CM000668.1:g.32170447T>C GRCh37
NC_000006.10:g.32278425T>C NCBI36
NG_028190.1:g.26398A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375023.3:c.3232-71A>G MANE Select ENSP00000364163.3:n.3232-71A>G
ENST00000474612.1:n.1247A>G
NM_004557.3:c.3232-71A>G NP_004548.3:n.3232-71A>G
NR_134949.1:n.3472+1100A>G
NR_134950.1:n.3370+1100A>G
NM_004557.4:c.3232-71A>G MANE Select NP_004548.3:n.3232-71A>G
NR_134949.2:n.3472+1100A>G
NR_134950.2:n.3370+1100A>G